Rosanna Weksberg

28.3k total citations · 1 hit paper
235 papers, 11.2k citations indexed

About

Rosanna Weksberg is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rosanna Weksberg has authored 235 papers receiving a total of 11.2k indexed citations (citations by other indexed papers that have themselves been cited), including 154 papers in Genetics, 152 papers in Molecular Biology and 80 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rosanna Weksberg's work include Epigenetics and DNA Methylation (84 papers), Genetic Syndromes and Imprinting (83 papers) and Prenatal Screening and Diagnostics (51 papers). Rosanna Weksberg is often cited by papers focused on Epigenetics and DNA Methylation (84 papers), Genetic Syndromes and Imprinting (83 papers) and Prenatal Screening and Diagnostics (51 papers). Rosanna Weksberg collaborates with scholars based in Canada, United States and United Kingdom. Rosanna Weksberg's co-authors include Sanaa Choufani, Cheryl Shuman, Anne S. Bassett, Daria Grafodatskaya, Eva W.C. Chow, Darci T. Butcher, Adam C. Smith, J. Bruce Beckwith, Y. Ann Chen and Jeremy A. Squire and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Rosanna Weksberg

232 papers receiving 11.0k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray

2013 983 citations Sanaa Choufani, Darci T. Butcher et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Rosanna Weksberg Canada	55	7.2k	5.5k	3.1k	980	966	235	11.2k
Maximilian Muenke United States	67	10.5k 1.5×	8.1k 1.5×	2.0k 0.6×	802 0.8×	1.4k 1.4×	277	15.6k
Valérie Cormier‐Daire France	62	8.4k 1.2×	7.2k 1.3×	1.0k 0.3×	1.2k 1.3×	1.3k 1.4×	393	14.3k
David Chitayat Canada	55	4.8k 0.7×	3.3k 0.6×	3.1k 1.0×	867 0.9×	1.9k 2.0×	403	11.6k
Carolyn A. Bondy United States	67	5.6k 0.8×	5.1k 0.9×	1.4k 0.4×	1.0k 1.0×	1000 1.0×	184	14.8k
Merlin G. Butler United States	60	5.8k 0.8×	10.4k 1.9×	3.0k 1.0×	419 0.4×	1.5k 1.6×	382	14.5k
Michel Vekemans France	44	4.1k 0.6×	3.3k 0.6×	1.7k 0.5×	901 0.9×	1.2k 1.3×	248	8.7k
Claus Højbjerg Gravholt Denmark	61	5.8k 0.8×	8.2k 1.5×	1.2k 0.4×	979 1.0×	1.2k 1.3×	316	13.3k
André Reis Germany	60	7.7k 1.1×	4.4k 0.8×	866 0.3×	401 0.4×	566 0.6×	320	13.6k
A. Joseph D’Ercole United States	57	5.2k 0.7×	2.7k 0.5×	1.7k 0.6×	798 0.8×	1.6k 1.6×	144	12.8k
Ethylin Wang Jabs United States	58	8.6k 1.2×	7.9k 1.4×	696 0.2×	660 0.7×	1.2k 1.3×	243	14.7k

Countries citing papers authored by Rosanna Weksberg

Since Specialization

Citations

This map shows the geographic impact of Rosanna Weksberg's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Rosanna Weksberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rosanna Weksberg more than expected).

Fields of papers citing papers by Rosanna Weksberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rosanna Weksberg. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Rosanna Weksberg. The network helps show where Rosanna Weksberg may publish in the future.

Co-authorship network of co-authors of Rosanna Weksberg

This figure shows the co-authorship network connecting the top 25 collaborators of Rosanna Weksberg. A scholar is included among the top collaborators of Rosanna Weksberg based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Rosanna Weksberg. Rosanna Weksberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Quach, Henry, Amy P. Wong, Anne L. Wheeler, et al.. (2025). Il-6 knockout reduces doxorubicin-induced toxicity in the developing mouse brain. Brain Behavior and Immunity. 129. 609–619.

Hansford, Jordan R., Anirban Das, Rose B. McGee, et al.. (2024). Update on Cancer Predisposition Syndromes and Surveillance Guidelines for Childhood Brain Tumors. Clinical Cancer Research. 30(11). 2342–2350. 9 indexed citations

Choufani, Sanaa & Rosanna Weksberg. (2024). P837: DNA methylation profiling in Kabuki syndrome: Steps towards improved classification of variants of uncertain significance. SHILAP Revista de lepidopterología. 2. 101748–101748.

Brzezinski, Jack, Gaëlle Bougeard, Garrett M. Brodeur, et al.. (2024). Update on Surveillance Guidelines in Emerging Wilms Tumor Predisposition Syndromes. Clinical Cancer Research. 31(1). 18–24. 2 indexed citations

Kalish, Jennifer M., Gaëlle Bougeard, Garrett M. Brodeur, et al.. (2024). Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith–Wiedemann Syndrome and Other Predisposition Syndromes. Clinical Cancer Research. 30(23). 5260–5269. 9 indexed citations

Bareke, Eric, Sanaa Choufani, Sujatha Jagadeesh, et al.. (2024). A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage. Molecular Genetics & Genomic Medicine. 12(2). e2402–e2402. 1 indexed citations

Awamleh, Zain, et al.. (2024). ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3. BMC Medical Genomics. 17(1). 282–282. 2 indexed citations

Shen, Yaoqing, Katherine Dixon, Andrew Galbraith, et al.. (2024). Long-read sequencing for detection and subtyping of Prader-Willi and Angelman syndromes. Journal of Medical Genetics. 62(1). 32–36. 2 indexed citations

Kamihara, Junne, Lisa Diller, William D. Foulkes, et al.. (2024). Neuroblastoma Predisposition and Surveillance—An Update from the 2023 AACR Childhood Cancer Predisposition Workshop. Clinical Cancer Research. 30(15). 3137–3143. 6 indexed citations

10.

Zhou, Yuqing, Darci T. Butcher, Rosanna Weksberg, et al.. (2018). Brain Development and Heart Function after Systemic Single-Agent Chemotherapy in a Mouse Model of Childhood Leukemia Treatment. Clinical Cancer Research. 24(23). 6040–6052. 12 indexed citations

11.

Fauth, Christine, Katharina Steindl, Annick Toutain, et al.. (2015). A recurrent germline mutation in the PIGA gene causes Simpson‐Golabi‐Behmel syndrome type 2. American Journal of Medical Genetics Part A. 170(2). 392–402. 30 indexed citations

12.

Butcher, Darci T., Rajat Singhania, Carolyn Β. Mervis, et al.. (2015). Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23. The American Journal of Human Genetics. 97(2). 216–227. 49 indexed citations

13.

Shugar, Andrea, et al.. (2015). An increased prevalence of thyroid disease in children with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 167(7). 1560–1564. 15 indexed citations

14.

Han, Kihoon, Vincenzo A. Gennarino, Yoontae Lee, et al.. (2013). Human-specific regulation of MeCP2 levels in fetal brains by microRNA miR-483-5p. Genes & Development. 27(5). 485–490. 86 indexed citations

15.

Inbar‐Feigenberg, Michal, Sanaa Choufani, Darci T. Butcher, Maian Roifman, & Rosanna Weksberg. (2013). Basic concepts of epigenetics. Fertility and Sterility. 99(3). 607–615. 117 indexed citations

16.

Choufani, Sanaa, Cheryl Shuman, & Rosanna Weksberg. (2013). Molecular Findings in Beckwith–Wiedemann Syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 163(2). 131–140. 139 indexed citations

17.

Mullegama, Sureni V., Christian R. Marshall, Anath C. Lionel, et al.. (2011). Severe intellectual disability and autistic features associated with microduplication 2q23.1. European Journal of Human Genetics. 20(4). 398–403. 27 indexed citations

18.

Li, Madeline, Cheryl Shuman, Eva Maria Cutiongco, et al.. (2001). GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome. American Journal of Medical Genetics. 102(2). 161–168. 87 indexed citations

19.

Lin, Angela E., et al.. (1999). Cardiac anomalies in the Simpson-Golabi-Behmel syndrome. American Journal of Medical Genetics. 83(5). 378–381. 52 indexed citations

20.

Squire, Jeremy A., et al.. (1998). Developmental Biology: Frontiers for Clinical Genetics: Overgrowth syndromes and genomie imprinting: from mouse to man. Clinical Genetics. 53(3). 165–170. 27 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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